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Details
Link-It Detail - Disease - Hypocalcemia
Debug Stats
  • ### Total Build Time: 397 ms 39.335 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 264 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=19 ms Completed: 19 ms rowSize= 1,009 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 544 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=17 ms Completed: 17 ms rowSize= 2.819 KB
  • CONCEPT_RELATIONSHIPS gt=298 ms Completed: 298 ms rowSize= 13.730 KB
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 19.339 KB
  • CONCEPT_XREFS gt=15 ms Completed: 15 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypocalcemia C0020598
Definition (1)
A disorder characterized by laboratory test results that indicate a low concentration of calcium in the blood.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Water-Electrolyte Imbalance C0043065
img Calcium Metabolism Disorders C0006705
Children (1)
img Tetany C0039621
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Water-Electrolyte Imbalance C0043065
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Calcium Metabolism Disorders C0006705
Relationships (107)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 73
diso_​to_​diso : 30
diso_​to_​phen : 2


Relationships:
none : 33
classifies : 2
disease_​may_​have_​finding : 1
induces : 1
isa : 7
mapped_​to : 2
may_​treat : 60
use : 1
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT124img In Blood C0005768
DISO_to_CHEM96img Calcium C0006675
DISO_to_DISO88img Complication Aspects C1171258
DISO_to_CHEM72img Calcium C0006675
DISO_to_ANAT71img In Blood C0005768
DISO_to_DISO68img chemically induced C0007994
DISO_to_DISO65img Complication Aspects C1171258
DISO_to_CHEM61img Parathyroid Hormone C0030520
DISO_to_DISO56img chemically induced C0007994
DISO_to_DISO43img Hypoparathyroidism C0020626
DISO_to_CHEM41img Parathyroid Hormone C0030520
DISO_to_DISO37img COMPL POSTOP C0032787
DISO_to_DISO35img Hypoparathyroidism C0020626
DISO_to_PHEN32img genetic aspects C0017399
DISO_to_DISO29img AVITAMINOSIS D C0042870
DISO_to_PHEN29img genetic aspects C0017399
DISO_to_DISO26img Hypercalcemia C0020437
DISO_to_DISO26img Thyroid Diseases C0040128
DISO_to_CHEM24img Diphosphonates C0012544
DISO_to_DISO22img CALCIUM BLOOD INCREASED C0020437
DISO_to_CHEM21img Vitamin D C0042866
DISO_to_DISO21img COMPL POSTOP C0032787
DISO_to_CHEM17img Bone Density Conservation Agents C1563726
DISO_to_CHEM17img Diphosphonates C0012544
DISO_to_DISO17img AVITAMINOSIS D C0042870
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
img OMIM, Score=1000, UMLKSK CUI: C0020598
img GENERIF, Score=861, Pubmed Id: 17217065, UMLKSK CUI: C0020598
img GENERIF, Score=861, Pubmed Id: 12032568, UMLKSK CUI: C0020598
img GENERIF, Score=861, Pubmed Id: 16075242, UMLKSK CUI: C0020598
HumanOSTM128962osteopetrosis associated transmembrane protein 1
INFERRED, Score=800, UMLKSK CUI: C0020598
HumanCLDN1610686claudin 16
INFERRED, Score=800, UMLKSK CUI: C0020598
HumanTCIRG110312T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
INFERRED, Score=800, UMLKSK CUI: C0020598
HumanGCM29247glial cells missing homolog 2 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img OMIM, Score=1000, UMLKSK CUI: C0020598
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanTBCE6905tubulin folding cofactor E
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanTBX16899T-box 1
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0020598
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
INFERRED, Score=800, UMLKSK CUI: C0020598
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanPTH5741parathyroid hormone
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
INFERRED, Score=800, UMLKSK CUI: C0020598
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanHLA-DQA13117
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanGNAS2778GNAS complex locus
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanCYP27B11594cytochrome P450, family 27, subfamily B, polypeptide 1
img OMIM, Score=1000, UMLKSK CUI: C0020598
img OMIM, Score=1000, UMLKSK CUI: C0020598
HumanCLCN71186chloride channel, voltage-sensitive 7
INFERRED, Score=800, UMLKSK CUI: C0020598
HumanCASR846calcium-sensing receptor
img GENERIF, Score=861, Pubmed Id: 15960151, UMLKSK CUI: C0020598
img OMIM, Score=1000, UMLKSK CUI: C0020598
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020598Hypocalcemia0self